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rs281860543

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860543(C;C)
Make rs281860543(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271095
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860543
ebirs281860543
HLIrs281860543
Exacrs281860543
Varsomers281860543
Maprs281860543
PheGenIrs281860543
hapmaprs281860543
1000 genomesrs281860543
hgdprs281860543
ensemblrs281860543
gopubmedrs281860543
geneviewrs281860543
scholarrs281860543
googlers281860543
pharmgkbrs281860543
gwascentralrs281860543
openSNPrs281860543
23andMers281860543
23andMe allrs281860543
SNP Nexus

SNPshotrs281860543
SNPdbers281860543
MSV3drs281860543
GWAS Ctlgrs281860543
Max Magnitude0
ClinVar
Risk rs281860543(C;C)
Alt rs281860543(C;C)
Reference rs281860543(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238872C>G
CLNSRC
CLNACC